SPIN4

spindlin family member 4
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber SPIN4 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • ?Lui-Jee-Baron syndrome, OMIM:301114